Journal of Agricultural and Food Chemistry · 2020 · 27 citations · 39 references
Life SciencesBiochemistryPlant SciencesCarbohydrate BiochemistryGlycobiologyPlant BiochemistryCarbohydrate StructureCell Wall StructureGlycan AnalysisGlycan DegradationPlant Cell Wall PolysaccharidesPolysaccharide StructureCellulose DegradationEnzymatic Cell Wall DegradationEnzymatic DegradationEnzymatic Polysaccharide DegradationLignocellulose DegradationPlant Cell Wall CompositionPlant Cell Wall DegradationPlant Cell Wall Polysaccharide Degradation
The study used mass spectrometry imaging (MSI) to map the distribution of enzymatically degraded cell wall polysaccharides in maize stems for two genotypes and at several stages of development. The context was the production of biofuels, and the overall objective was to better describe the structural determinants of recalcitrance of grasses in bioconversion. The selected genotypes showed contrasting characteristics in bioconversion assays as well as in their lignin deposition pattern. We compared the pattern of cell wall polysaccharide degradation observed by MSI following the enzymatic degradation of tissues with that of lignin deposition. Several enzymes targeting the main families of wall polysaccharides were used. In the early stages of development, cellulose and mixed-linked β-glucans appeared as the main polysaccharides degraded from the walls, while heteroxylan products were barely detected, suggesting subsequent deposition of heteroxylans in the walls. At all stages and for both genotypes, enzymatic degradation occurred preferentially in nonlignified walls for all structural families of polysaccharides studied here. However, our results showed heterogeneity in the distribution of heteroxylan products according to their chemical structure: arabinosylated products were mostly represented in the pith center, while glucuronylated products were found at the pith periphery. The conclusions of our work are in agreement with those of previous studies. The MSI approach presented here is unique and attractive for addressing the histological and biochemical aspects of biomass recalcitrance to conversion, as it allows for a simultaneous interpretation of cell wall degradation and lignification patterns at the scale of an entire stem section.
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